Jamel Chelly

10.8k citations

110 papers · 5.3k indexed · 1 hit paper · h-index 38

Molecular Biology top 2%
Genetics top 0.2%
Cognitive Neuroscience top 2%
Cellular and Molecular Neuroscience top 2%
Cell Biology top 2%

Co-authors: Thierry Bienvenu Claude Moraine Hans‐Hilger Ropers Martine Raynaud Ben C.J. Hamel Chérif Beldjord Jean‐Pierre Fryns Juliette Nectoux
Topics: Genetics and Neurodevelopmental Disorders (92 papers)Genomic variations and chromosomal abnormalities (24 papers)RNA modifications and cancer (19 papers)
Cited by: Genetics Developmental Neuroscience Cognitive Neuroscience
Journals: Proceedings of the National Academy of Sciences Nature Genetics Journal of Neuroscience
Partner nations: France Germany Netherlands

In The Last Decade

Jamel Chelly

110 papers receiving 5.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family

2004 553 citations Frédéric Laumonnier, Frédérique Bonnet‐Brilhault et al. The American Journal of Human Genetics profile →

Peers

Countries citing papers authored by Jamel Chelly

Since Specialization

Citations

This map shows the geographic impact of Jamel Chelly's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jamel Chelly with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jamel Chelly more than expected).

Fields of papers citing papers by Jamel Chelly

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jamel Chelly. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jamel Chelly. The network helps show where Jamel Chelly may publish in the future.

Co-authorship network of co-authors of Jamel Chelly

This figure shows the co-authorship network connecting the top 25 collaborators of Jamel Chelly. A scholar is included among the top collaborators of Jamel Chelly based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jamel Chelly. Jamel Chelly is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Expanding the clinical phenotype of patients with a ZDHHC9 mutation 2013 ·American Journal of Medical Genetics Part A ·Alice Masurel‐Paulet,Vera M. Kalscheuer,Nicolas Lebrun,Hao Hu,(unknown),Christel Thauvin‐Robinet,Véronique Darmency‐Stamboul,Salima El Chehadeh,Julien Thévenon,(unknown),(unknown),(unknown),Jean‐Michel Pinoit,Frédéric Huet,Vincent Desportes,Jamel Chelly,Laurence Faivre	28
2	Custom oligonucleotide array-based CGH: a reliable diagnostic tool for detection of exonic copy-number changes in multiple targeted genes 2013 ·European Journal of Human Genetics ·(unknown),(unknown),(unknown),(unknown),Aurélie Toussaint,Chrystel Leroy,(unknown),(unknown),Nathalie Deburgrave,Yoann Saillour,(unknown),Corinne Fouveaut,Chérif Beldjord,Sophie Valleix,France Leturcq,Catherine Dodé,Thierry Bienvenu,Jamel Chelly,Mireille Cossée	14
3	Cell cloning‐based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes 2010 ·Journal of Cellular and Molecular Medicine ·Juliette Nectoux,Yann Fichou,Haydeé Rosas‐Vargas,Nicolas Cagnard,Nadia Bahi‐Buisson,Patrick Nusbaum,Franck Letourneur,Jamel Chelly,Thierry Bienvenu	27
4	Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant 2009 ·Neurogenetics ·Nadia Bahi‐Buisson,Juliette Nectoux,Benôıt Girard,Hilde Van Esch,Thomy de Ravel,Nathalie Boddaert,Perrine Plouin,Marlène Rio,Yann Fichou,Jamel Chelly,Thierry Bienvenu	57
5	Cell-Autonomous Roles of ARX in Cell Proliferation and Neuronal Migration during Corticogenesis 2008 ·Journal of Neuroscience ·Gaëlle Friocourt,Shigeaki Kanatani,Hidenori Tabata,Masato Yozu,Takao Takahashi,(unknown),Odile Raguénès,Jamel Chelly,Claude Férec,Kazunori Nakajima,John G. Parnavelas	90
6	X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11 2006 ·European Journal of Human Genetics ·Lars Riff Jensen,Steffen Lenzner,Bettina A. Moser,Kristine Freude,Andreas Tzschach,Wei Chen,Jean‐Pierre Fryns,Jamel Chelly,Gillian Turner,Claude Moraine,Ben C.J. Hamel,Hans‐Hilger Ropers,Andreas W. Kuß	12
7	G.P.6 02 Somatic and germinal mosaicism of an out-of-frame deletion in the dystrophin gene in an adult male patient with predominant dilated cardiomyopathy 2006 ·Neuromuscular Disorders ·Yanyan Hu,France Leturcq,D. Héron,Delphine Logeart‐Avramoglou,S. Llense,Jamel Chelly,Dominique Récan,(unknown),(unknown),B. Eymard	1
8	The ARX mutations: A frequent cause of X‐linked mental retardation 2006 ·American Journal of Medical Genetics Part A ·Magdalena Nawara,Krzysztof Szczałuba,Karine Poirier,Krystyńa Chrzańowska,Jacek Pilch,Jerzy Bal,Jamel Chelly,Tadeusz Mazurczak	29
9	Retards mentaux liés à l’X 2005 ·médecine/sciences ·Pierre Billuart,Jamel Chelly,S Gilgenkrantz	4
10	Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update 2005 ·European Journal of Medical Genetics ·Christophe Philippe,Laurent Villard,Nicolás de Roux,Martine Raynaud,(unknown),Laurent Pasquier,Gaëtan Lesca,Julien Mancini,Philippe Jonveaux,A. Moncla,Jamel Chelly,Thierry Bienvenu	57
11	X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian family 2005 ·European Journal of Medical Genetics ·Hilde Van Esch,Ginevra Zanni,Maureen Holvoet,Martine Borghgraef,Jamel Chelly,Jean‐Pierre Fryns,Koenraad Devriendt	8
12	Screening of ARX in mental retardation families: consequences for the strategy of molecular diagnosis 2005 ·Neurogenetics ·Karine Poirier,Didier Lacombe,Brigitte Gilbert‐Dussardier,Martine Raynaud,Vincent Desportes,Arjan P.M. de Brouwer,Claude Moraine,J P Fryns,Hans‐Hilger Ropers,C. Beldjord,Jamel Chelly,Thierry Bienvenu	32
13	X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Familybreakdown → 2004 ·The American Journal of Human Genetics ·Frédéric Laumonnier,Frédérique Bonnet‐Brilhault,Marie Gomot,Romuald Blanc,Albert David,Marie‐Pierre Moizard,Martine Raynaud,Nathalie Ronce,Éric Lemonnier,Patrick Calvas,Béatrice Laudier,Jamel Chelly,Jean‐Pierre Fryns,Hans‐Hilger Ropers,Ben C.J. Hamel,Christian Andrés,Catherine Barthélémy,Claude Moraine,Sylvain Briault	553
14	Mutations in the ZNF41 Gene Are Associated with Cognitive Deficits: Identification of a New Candidate for X-Linked Mental Retardation 2003 ·The American Journal of Human Genetics ·Sarah A. Shoichet,Kirsten Hoffmann,Corinna Menzel,Udo Trautmann,Bettina A. Moser,Maria Hoeltzenbein,Bernard Échenne,M. W. Partington,Hans van Bokhoven,Claude Moraine,Jean‐Pierre Fryns,Jamel Chelly,Hans‐Dieter Rott,Hans‐Hilger Ropers,Vera M. Kalscheuer	65
15	Spectrum of MECP2 Mutations in Rett Syndrome 2002 ·Genetic Testing ·Thierry Bienvenu,Laurent Villard,Nicolás de Roux,Violaine Bourdon,Michel Fontés,Chérif Beldjord,Marc Tardieu,Philippe Jonveaux,Jamel Chelly	14
16	Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy 2001 ·Human Mutation ·Thierry Bienvenu,Isabelle Souville,Karine Poirier,(unknown),Lydie Bürglen,Jeanne Amiel,Bénédicte Héron,Anna Kamińska,Philippe Couvert,Chérif Beldjord,Jamel Chelly	8
17	Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54) 1999 ·American Journal of Medical Genetics ·Lamia Ben Jemâa,Vincent des Portes,Ramzi Zemni,Ridha Mrad,Faouzi Mâazoul,C. Beldjord,Habiba Chaâbouni,Jamel Chelly	7
18	Construction of a YAC contig spanning the Xq13.3 subband 1995 ·Genomics ·Laurent Villard,Jozef Gécz,Laurence Colleaux,Anne-Marie Lossi,Jamel Chelly,Yumiko Ishikawa-Brush,Anthony P. Monaco,Michel Fontés	16
19	7 Menkes and Wilson Diseases 1995 ·Advances in genetics ·Anthony P. Monaco,Jamel Chelly	6
20	Assignment of the gene (EPLG2) encoding a high-affinity binding protein for the receptor tyrosine kinase Elk to a 200-kilobasepair region in human chromosome Xq12 1995 ·Genomics ·Frederick A. Fletcher,Kay Huebner,Lisa G. Shaffer,(unknown),Anthony P. Monaco,Ulrich Müller,Teresa Druck,(unknown),Jamel Chelly,John W. Belmont,M P Beckmann,Stewart D. Lyman	9

About Jamel Chelly

Jamel Chelly is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience, having authored 110 papers that have together received 5.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (92 papers), Genomic variations and chromosomal abnormalities (24 papers) and RNA modifications and cancer (19 papers). The work is most often cited by research in Genetics (3.3k citations), Developmental Neuroscience (309 citations) and Cognitive Neuroscience (1.0k citations). Jamel Chelly has collaborated with scholars based in France, Germany and Netherlands. Frequent co-authors include Thierry Bienvenu, Claude Moraine, Hans‐Hilger Ropers, Martine Raynaud, Ben C.J. Hamel, Chérif Beldjord, Jean‐Pierre Fryns, Juliette Nectoux, Fiona Francis and Nathalie Ronce. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Journal of Neuroscience.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact